Ontology highlight
ABSTRACT: Background
Despite the development of several FLT3 inhibitors that have improved outcomes in patients with FLT3-mutant acute myeloid leukemias (AML), drug resistance is frequently observed, which may be associated with the activation of additional pro-survival pathways such as those regulated by BTK, aurora kinases, and potentially others in addition to acquired tyrosine kinase domains (TKD) mutations of FLT3 gene. FLT3may not always be a driver mutation.Objective
To evaluate the anti-leukemia efficacy of the novel multi-kinase inhibitor CG-806, which targets FLT3 and other kinases, in order to circumvent drug resistance and target FLT3 wild-type (WT) cells.Methods
The anti-leukemia activity of CG-806 was investigated by measuring apoptosis indu
SUBMITTER: Yu G
PROVIDER: S-EPMC9980215 | biostudies-literature | 2023 Feb
REPOSITORIES: biostudies-literature